Dear Editor, In 2017 our team published a meta-analysis on the health outcomes of offspring conceived from donor sperm.1 At the time of this review, there were only eight studies that were eligible for inclusion, and only three qualified for meta-analysis, 2-4 and only two studies provided data for each outcome analysis. Our review demonstrated the paucity of studies investigating the perinatal outcomes of sperm donation.After identifying this gap in research, we undertook a population study comparing the perinatal outcomes for neonates conceived with donor sperm and those conceived spontaneously in the state of South Australia.5 Furthermore, since the census date of the metaanalysis a further two studies have been published that also meet the criteria of our original review, 6,7 and we believed it was important that we add these three studies (two by other authors and one by ourselves), to our meta-analysis to see if the original findings were either supported or refuted.The original findings showed that; donor sperm neonates in comparison to naturally conceived neonates were not at increased risk of being born of low birth weight [risk ratio (RR): 1.04, 95% confidence interval (CI): 0.86-1.25, P-value (P) = 0.71, I 2 = 0%]; preterm (RR: 0.91, CI: 0.75-1.12, P = 0.38, I 2 = 0%); or with increased incidences of birth defects (RR: 1.20, CI: 0.97-1.48, P = 0.09, I 2 = 57%).
1The addition of the new studies allowed not only for an increase in the number of studies included in the meta-analysis conducted above but also for a larger range of perinatal outcomes. All data extraction and analysis followed the method described in our original review. The studies that were included in each meta-analysis are listed as reference numbers in superscript after each meta-analysis.The updated meta-analysis has demonstrated that, in comparison to naturally conceived neonates, donor sperm neonates were at increased risk of being born of low birth weight (RR: 1.17, CI: 1.03-1.33, P = 0.02, I 2 = 52%), [3][4][5][6][7] and with increased incidences of birth defects (RR: 1.30, CI: 1.05-1.59, P = 0.01, I 2 = 72%) (Fig. 1). 2,4,6 However, they were not at increased risk of being born preterm (RR: 1.05, CI: 0.91-1.21, P = 0.47, I 2 = 52%), [3][4][5]7 very preterm (<32 weeks) (RR: 1.17, CI: 0.75-1.81, P = 0.49, I 2 = 0%), 5,7 very low birth weight (<1500 g) (RR: 1.22, CI: 0.76-1.97, P = 0.4, I 2 = 0%), 5,7 small for gestational age (birth weight <10th percentile) (RR: 1.19, CI: 0.99-1.42, P = 0.06, I 2 = 82%), 5,7 large for gestational age (birth weight > 90th percentile) (RR: 1.04, CI: 0.86-1.38, P = 0.71, I 2 = 0%), 5,7 with altered perinatal mortality (RR: 0.93, CI: 0.59-1.45, P = 0.74, I 2 = 0%), 5,7 of lower mean birth weight (mean difference −12.5 g, CI: −32.03 to 7.02 g, P = 0.21, I 2 = 0%), 3,[5][6][7] or of lower mean gestational age (mean difference −0.02 weeks, CI: −0.10 to 0.05 weeks, P = 0.55, I 2 = 12%). 5,7